USA - Technical Writer - II - USD (contract)
Technical Writing, Author method validation documents.
This role will provide non-testing support to the QC Product Technical Support department.
This scope includes coordination of generating validation documents to support product validation at the Pfizer Andover site. The technical skills within scope will require understanding of the scientific principles of test methods, data analysis and cGMP requirement. The candidate will be responsible for facilitating lifecycle management through collaboration with laboratory subject matter experts (SMEs) and analysts at Pfizer.
The key responsibilities of the candidate are as follows:
Authoring method validation documents using Pfizer document workflow, through collaboration with SMEs Use of the Laboratory Management System (LIMS) Supporting assay improvement activities and generating supporting documents.
Participating in across site meetings and tracking the project timeline Successful candidate requires: Knowledge of QC microbial support and technical writing Strong interpersonal and written communication skills
A detail-oriented approach to deliverables as the main job responsibility is data review and generation of GMP documentation A degree in science, preferably in microbiology or related technical discipline Past experience supporting GMP writing in the biopharmaceutical field
Pay Rate Range
50 - 57 USD hourly
Additional Notes
Please note that contractors are engaged to provide services to Pfizer on a temporary basis in connection with a specific assignment. Contractors are hired and employed through Atrium, our third-party payrolling partner.
Benefits Information
This job posting is for a temporary role as an employee of Atrium on assignment at Pfizer. The individual selected for this role will be offered the role as an employee of Atrium; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by Atrium upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.
Benefits Information
Comprehensive Benefits Package available based on eligibility
• Medical, Dental, Vision
• Short-Term Disability (STD)
• Long-Term Disability (LTD)
• Supplemental and Voluntary Life Insurance
• 401(K)
• Commuter Benefit Program
Apply Now
Apply Now
This role will provide non-testing support to the QC Product Technical Support department.
This scope includes coordination of generating validation documents to support product validation at the Pfizer Andover site. The technical skills within scope will require understanding of the scientific principles of test methods, data analysis and cGMP requirement. The candidate will be responsible for facilitating lifecycle management through collaboration with laboratory subject matter experts (SMEs) and analysts at Pfizer.
The key responsibilities of the candidate are as follows:
Authoring method validation documents using Pfizer document workflow, through collaboration with SMEs Use of the Laboratory Management System (LIMS) Supporting assay improvement activities and generating supporting documents.
Participating in across site meetings and tracking the project timeline Successful candidate requires: Knowledge of QC microbial support and technical writing Strong interpersonal and written communication skills
A detail-oriented approach to deliverables as the main job responsibility is data review and generation of GMP documentation A degree in science, preferably in microbiology or related technical discipline Past experience supporting GMP writing in the biopharmaceutical field
Pay Rate Range
50 - 57 USD hourly
Additional Notes
Please note that contractors are engaged to provide services to Pfizer on a temporary basis in connection with a specific assignment. Contractors are hired and employed through Atrium, our third-party payrolling partner.
Benefits Information
This job posting is for a temporary role as an employee of Atrium on assignment at Pfizer. The individual selected for this role will be offered the role as an employee of Atrium; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by Atrium upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.
Benefits Information
Comprehensive Benefits Package available based on eligibility
• Medical, Dental, Vision
• Short-Term Disability (STD)
• Long-Term Disability (LTD)
• Supplemental and Voluntary Life Insurance
• 401(K)
• Commuter Benefit Program
Apply Now
Apply Now